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rs121964860

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964860(G;T)
Make rs121964860(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position201361988
GeneTNNT2
is asnp
is mentioned by
dbSNPrs121964860
ebirs121964860
HLIrs121964860
Exacrs121964860
Varsomers121964860
Maprs121964860
PheGenIrs121964860
hapmaprs121964860
1000 genomesrs121964860
hgdprs121964860
ensemblrs121964860
gopubmedrs121964860
geneviewrs121964860
scholarrs121964860
googlers121964860
pharmgkbrs121964860
gwascentralrs121964860
openSNPrs121964860
23andMers121964860
23andMe allrs121964860
SNP Nexus

SNPshotrs121964860
SNPdbers121964860
MSV3drs121964860
GWAS Ctlgrs121964860
Max Magnitude0
OMIM191045
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121964860(A,C,T;A,C,T)
Alt rs121964860(A,C,T;A,C,T)
Reference rs121964860(G;G)
Significance Pathogenic
Disease Left ventricular noncompaction 6 not specified
Variation info
Gene TNNT2
CLNDBN Left ventricular noncompaction 6 not specified
Reversed 1
HGVS NC_000001.10:g.201331116C>A; NC_000001.10:g.201331116C>G; NC_000001.10:g.201331116C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013228.24, RCV000220074.1, RCV000152098.1,